QUÍMICA ORGÁNICA SINTÉTICA Y CATÁLISIS
QOSCAT
University of Cambridge
Cambridge, Reino UnidoPublicaciones en colaboración con investigadores/as de University of Cambridge (15)
2015
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An Autocatalytic System of Photooxidation-Driven Substitution Reactions on a FeII4L6 Cage Framework
Angewandte Chemie - International Edition, Vol. 54, Núm. 48, pp. 14378-14382
2014
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Fluorophore incorporation allows nanomolar guest sensing and white-light emission in M4L6 cage complexes
Chemical Science, Vol. 5, Núm. 3, pp. 908-915
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Selective encapsulation and sequential release of guests within a self-sorting mixture of three tetrahedral cages
Angewandte Chemie - International Edition, Vol. 53, Núm. 18, pp. 4556-4560
2012
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Integrative self-sorting synthesis of a Fe8Pt6L 24 cubic cage
Angewandte Chemie - International Edition, Vol. 51, Núm. 27, pp. 6681-6685
2005
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Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives
Organic and Biomolecular Chemistry, Vol. 3, Núm. 22, pp. 4095-4107
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Total synthesis of the Fusarium toxin equisetin
Organic and Biomolecular Chemistry, Vol. 3, Núm. 2, pp. 274-280
2004
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Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides
Organic and Biomolecular Chemistry, Vol. 2, Núm. 24, pp. 3618-3627
2003
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The Use of Butane Diacetals of Glycolic Acid as Precursors for the Synthesis of the Phytotoxic Calmodulin Inhibitor Herbarumin II
Helvetica Chimica Acta, Vol. 86, Núm. 11, pp. 3717-3729
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Total synthesis of the phytotoxic agent herbarumin II using butane diacetals of glycolic acid as building blocks
Synlett, pp. 1186-1188
2002
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Highly diastereoselective ketone aldol reactions of butane-2,3-diacetal desymmetrised glycolic acid
Synthesis, pp. 1973-1978
2001
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A new phase-switch method for application in organic synthesis programs employing immobilization through metal-chelated tagging
Angewandte Chemie - International Edition, Vol. 40, Núm. 6, pp. 1053-1055
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Consecutive three- and four-component coupling reactions with anions generated from a butane diacetal desymmetrized glycolic acid derivative
Angewandte Chemie - International Edition, Vol. 40, Núm. 24, pp. 4763-4765
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Highly diastereoselective Michael addition reactions of butane-2,3-diacetal desymmetrized glycolic acid. Preparation of α-hydroxy-γ-amino acid derivatives
Organic Letters, Vol. 3, Núm. 23, pp. 3753-3755
2000
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A short stereoselective total synthesis of the fusarium toxin equisetin
Organic Letters, Vol. 2, Núm. 23, pp. 3611-3613
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Deracemization of Baylis-Hillman adducts
Chemtracts, Vol. 13, Núm. 9, pp. 596-601